Canonical Allele Identifier: CA472909794

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6413219C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6391989C>T , CM000673.2:g.6391989C>T	GRCh38
NC_000011.9:g.6413219C>T , CM000673.1:g.6413219C>T	GRCh37
NC_000011.8:g.6369795C>T	NCBI36
NG_011780.1:g.6565C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.924C>T MANE Select	ENSP00000340409.4:p.Phe308=
ENST00000342245.8:c.924C>T	ENSP00000340409.4:p.Phe308=
ENST00000526280.1:c.113C>T
ENST00000527275.5:c.921C>T	ENSP00000435350.1:p.Phe307=
ENST00000530395.1:c.105C>T	ENSP00000431479.1:p.Phe35=
ENST00000531303.5:c.438+486C>T	ENSP00000432625.1:n.438+486C>T
ENST00000533123.5:c.924C>T	ENSP00000435950.1:p.Phe308=
ENST00000533196.1:n.375-17C>T
ENST00000534405.5:c.924C>T	ENSP00000434353.1:p.Phe308=
NM_000543.4:c.924C>T	NP_000534.3:p.Phe308=
NM_001007593.2:c.921C>T	NP_001007594.2:p.Phe307=
XM_005253075.3:c.924C>T	XP_005253132.1:p.Phe308=
XM_011520303.1:c.924C>T	XP_011518605.1:p.Phe308=
XM_011520304.1:c.924C>T	XP_011518606.1:p.Phe308=
XR_930886.1:n.1222C>T
NM_001318087.1:c.924C>T	NP_001305016.1:p.Phe308=
NM_001318088.1:c.-38C>T	NP_001305017.1:n.-38C>T
NM_001365135.1:c.924C>T	NP_001352064.1:p.Phe308=
NR_027400.2:n.1109C>T
NR_134502.1:n.623+486C>T
XM_011520304.2:c.924C>T	XP_011518606.1:p.Phe308=
XR_001747940.2:n.1049C>T
XR_002957158.1:n.1049C>T
NM_000543.5:c.924C>T MANE Select	NP_000534.3:p.Phe308=
NM_001007593.3:c.921C>T	NP_001007594.2:p.Phe307=
NM_001318087.2:c.924C>T	NP_001305016.1:p.Phe308=
NM_001318088.2:c.-38C>T	NP_001305017.1:n.-38C>T
NM_001365135.2:c.924C>T	NP_001352064.1:p.Phe308=
NR_027400.3:n.1049C>T
NR_134502.2:n.563+486C>T